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INVITED ARTICLE Table of Contents   
Year : 2009  |  Volume : 51  |  Issue : 5  |  Page : 93-97
Closing the treatment gap for dementia in India


1 Epidemiologist and Geriatrician, Coordinator 10/66 Dementia Research Group - India, Jt. Secretary, Alzheimer's and Related Disorders Society of India, Department of Preventive and Social Medicine, Goa Medical College, Goa, India
2 Professor of International Mental Health, London School of Hygiene and Tropical Medicine, UK and Sangath, Goa, India

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   Abstract 

There is a rich epidemiological evidence base on dementia in India which shows that this neurodegenerative condition is an important public health problem, particularly in the context of the rapid demographic transition in many parts of the country. Research has shown that most people with dementia, and their caregivers, have significant unmet health and social welfare needs. Due to the great shortage of health care resources and the low levels of awareness about dementia, interventions addressing the needs of the people should be home based and directed at improving quality of life of the person with dementia and the caregiver. In view of the lack of specialists to deal with dementia, a group in Goa developed an alternate model of care which involved training lay health workers to provide home-based care for people with dementia under the supervision of a psychiatrist. This was successfully implemented and evaluated in a randomized controlled trial which showed clear benefits. This article concludes by considering the implication of these findings on strategies for scaling up services and close the treatment gap for dementia in India.

Keywords: Dementia, treatment gap, community based interventions, primary care

How to cite this article:
Dias A, Patel V. Closing the treatment gap for dementia in India. Indian J Psychiatry 2009;51, Suppl S1:93-7

How to cite this URL:
Dias A, Patel V. Closing the treatment gap for dementia in India. Indian J Psychiatry [serial online] 2009 [cited 2020 Nov 25];51, Suppl S1:93-7. Available from: https://www.indianjpsychiatry.org/text.asp?2009/51/5/93/44868



   Introduction Top


Understanding the burden of dementia is vital for developing and promoting dementia services in the Low and Middle Income Countries (LMICs). Other articles in this special issue of the IJP provide a systematic overview of the epidemiology of dementia in India. In 2005, the 10/66 dementia research group, estimated that there were 24.3 million people with dementia in the world which increase at the rate of 4.6 million every year [1] . The study also estimated that the prevalence of dementia in India and South Asia was 1.9% in those ≥60 years with an annual incidence of 4.3/1000. The prevalence is estimated to reach 3.6 million by 2020 and 7.5 million by 2040 in this region[1] . The rate of increase was estimated to be 3-4 times higher in developing countries than in developed countries. [1]

There are a number of essential issues which need to be addressed in planning services for people with dementia in India, as listed below:

  • What is the burden, in absolute numbers, of people affected?
  • What are the help-seeking patterns of people with dementia?
  • What is the estimated treatment gap for evidence based care?
  • How should evidence based services be delivered, by whom and in what settings?


Each of these will be discussed in this article, concluding with implications of this evidence base for closing the treatment gap for dementia.


   The Burden of Dementia in India Top


Since health is a state subject in India, it is important to estimate the burden of dementia in individual states of the country as a first step to planning services. Considering the prevalence of 1.9% cited earlier, we have estimated the numbers of persons with dementia in each states using the census 2001 data [2] as shown in [Table 1]. We estimate that there are, in total, nearly 1.5 million people living with dementia in India today. These numbers are expected to increase dramatically in the years ahead due to the demographic transition.


   Help-Seeking for People with Dementia Top


For most people, the features characteristic of dementia are considered to be part of, or a non-pathological deviation from, normal ageing. A study in Goa looked at the attitudes towards mental health problems in elders amongst health care providers and family caregivers. [3] Although a vignette of dementia was widely recognized, the condition was not thought to constitute a health problem. Dementia was construed as a normal part of ageing and was not perceived as requiring medical care. Thus, primary health physicians rarely saw this condition in their clinical work, but community health workers frequently recognized individuals with dementia. Indeed, there was no label in the local language for dementia. Dementia was occasionally attributed to abuse, neglect, or lack of love on the part of children towards a parent. There was evidence that the system of family care and support for older persons was less reliable than has been claimed. Care was often conditional upon the child's expectation of inheriting the parent's property. Care for those with dependency needs was almost entirely family-based with little or no formal services. Not surprisingly, fear for the future, and in particular 'dependency anxiety' was commonplace among older persons. There is stigma associated with the psychological and behavioral problems associated with dementia. People are often neglected in their homes and sometimes abused.

Formal care arrangements for elders, for example in the public health sector, are scarce. The specialities of old age psychiatry or geriatric medicine are very poorly established in the country and there is virtually no concept of continuing care which meets the complex medical and psychosocial needs of people with dementia and their families. [4] The number of residential places for elders with severe mental disorders such as dementia is also very low; the most recent estimate we could find is nearly 10 years old and reported about 354 homes, more than half of which were in the two southern states of Kerala and Tamil Nadu . Thus, the family remains not only the primary source of care and support for the vast majority of elders in India, but in fact the only source as well.

Caring for people with dementia is associated with a greater physical, mental, and financial burden on the caregiver. [5] Studies by the 10/66 Dementia Research Network in Goa and Chennai examined the impact of care giving for elders. Carers of people with dementia spent significantly longer time providing care than did carers and co-residents of depressed persons and controls. The highest proportion of time was spent in communicating, supervising, and helping with eating and toileting. They were much more likely to have a common mental disorder than carers or co-residents of controls. Economic strain was indicated by the high proportion of caregivers of people with dementia who had given up work to provide care, coupled with the increased likelihood that the family had to meet relatively high health care costs. This was explained by the increased propensity for people with dementia to use expensive private medical care services rather than free or low cost government services. [5]


   The Treatment GAP for Dementia in India Top


The concept of the treatment gap describes the gap between the numbers of people with a health condition and the number of these people who receive at least basic evidence based care. The recent Disease Control Priorities Project identified the effective treatments for dementia. [6] Anticholinesterase drugs show benefits only for patients with mild to moderate dementia, and only in the short term. However, the high costs of these drugs mean that these are unlikely to be cost-effective in low resource environments. Training family caregivers in behavioral management techniques reduces the level of agitation and anxiety in people with dementia. Use of low doses of antipsychotic medications, which reduce symptoms such as aggression and wandering, have been shown to reduce caregiver stress. Interventions that have specifically targeted stress and depression among caregivers are also beneficial.

There are no accurate estimates for the treatment gap for dementia in India, but we estimate that this gap exceeds 90% in most parts of the country, with the exception of urban areas and the two southern states of Kerala and Tamil Nadu. We do have relatively accurate estimates of the treatment gap from Goa. In a recent study in which 81 subjects with dementia participated, although 41 (51%) were seen by a doctor in the previous three months, only 4 (5%) had received the diagnosis and treatment specific for dementia. Thus, the treatment gap was over 90%, even in this relatively prosperous state of India with relatively good public health and mental health services. The study also reported that some families refused to take dementia specific medications mainly citing reasons including high cost, the family doctor advising not to take the medications, and fear of side effects. [7]

There are several major barriers to closing this treatment gap including the low levels of awareness about dementia as a medical disorder; however, the most significant barrier is the very low human resource capacity for the care of people with dementia. This scarcity of resources is true for all mental disorders across the continuum of life and has been systematically documented in the recent Lancet series on Global Mental Health. [8] India, like most LMICs, lack economic and human capital to achieve widespread coverage of specialist services; [9] furthermore, specialist services tend to focus almost entirely on medical interventions, which have only a limited role in the long-term care of people with dementia. In view of the above, service development for families of people with dementia in India should keep in mind that the service should be home based, address the diverse medical and psychosocial health needs of the affected persons and their caregivers and be provided at a cost that the family can afford (therefore use public and low-cost service providers). Thus, the challenge for India is to develop culturally appropriate interventions that can be delivered within existing resources, such as supporting families in their role as caregivers. The model of care in developing countries should be based on home care, along with providing training and support for family caregivers. [6] Interventions that should not be pursued include the use of multiple medications, which can be detrimental in older age groups, particularly unproven medications such as cerebral activators and neurotropic agents.


   Delivering Evidence based Services at a Low Cost: The Home Care Program Top


A randomized controlled trial has recently been completed in two talukas of Goa evaluating the benefits of a low-cost, home-based intervention aimed at supporting families affected by dementia. [7] The intervention was delivered by a community team, one for each taluka. Each team comprised two full-time Home Care Advisors (HCA), and a part-time local psychiatrist from the public health services, and a part-time lay counselor (who was shared by both teams). The minimum requirements for being a HCA were knowledge of the local language, being literate, preferably passed higher secondary school, and motivated to be involved in the community care of older people. They received intensive training for a week through role-play and interactive training methods. The HCA were trained in key skills including listening and counseling skills, bereavement counseling, stress management, and health advice for common health problems. The specific components of the intervention carried out by the HCA were:

  • Basic education about dementia (what is the disease, its course, its features, etc.).
  • Education about common behavior problems and how they can be managed.
  • Support to the caregiver, for example: for an elderly caregiver living alone with the patient, in activities of daily living.
  • Referral to psychiatrists or the family doctor when behavior problems are severe and warrant medication intervention.
  • Networking of families to enable the formation of support groups.
  • Advice regarding existing government schemes for elders.


The HCA applied a flexible home-care program tailored to the needs of the individual and the family. The minimum frequency of visits was at least once a fortnight for six months. The maximum was based on the needs as assessed by the HCA. Thus, the visits could be more frequent depending on the need of that particular family. The HCA were supported, and supervised, by the two part-time specialists: two psychiatrists (one supporting each team) and one counselor (supporting both teams; the counselor was herself a carer for a parent with dementia). Each person with dementia was seen at least once by a local psychiatrist who confirmed the diagnosis of dementia and advised regarding use of medication for behavior and other common medical problems based on an agreed protocol. The caregiver and the person with dementia were encouraged to visit the psychiatrist in the clinic so that, if medication or clinical investigations were needed, these could be availed of at no cost from the public health service, and because the time required for travel for the psychiatrist for home visits was considered to be wasting a precious resource. A home visit was arranged if a clinic visit was not possible. HCA would meet the psychiatrist twice a month and update them on the progress of the person with dementia, particularly those who were receiving medication. The other specialist was a lay counselor who had herself been a caregiver for a parent with dementia. The HCA from both talukas met with the counselor once a fortnight to share experiences, support one another, and solve difficult situations. Thus, the intervention followed a flexible stepped care model aimed at improving the knowledge of the family caregivers, providing emotional support, maximize caregiving resources and improving caregiving skills. The intervention demonstrated a significant impact in reducing the caregiver burden, mental stress, and distress due to the behavioral and psychological symptoms of dementia. It also showed a non-significant reduction in the total number of deaths in people with dementia in the intervention arm.


   Implications for Scaling up Services for Dementia in India Top


The Kyoto Declaration of the Alzheimer's Disease International (ADI) identifies the minimal actions required for dementia care in low, medium, and high resource settings. [10] This was based on the recommendations by the WHO 2001 [11] and is summarized in [Table 2]. The focus has been to integrate dementia services with the primary health care system. The Goa Home Care Program demonstrates that it is possible to introduce a community dementia outreach programme as part of the existing primary health care set up, relying on trained low-cost community health workers supervised by mental health or other appropriately trained specialists. We believe that it would not be ideal to involve the existing community health workers, such as multi- purpose workers for dementia care as they are already overburdened with programmes involving vector borne diseases, tuberculosis, reproductive and child health, immunizations, etc. However, there are a number of conditions which, like dementia, produce chronic disabilities (such as strokes) and which may benefit from community based psychosocial interventions. Thus, it is possible that the model of home based support we have developed may be extended to such conditions to create a 'chronic disease counselor' whose primary role is to support persons (and families) affected by chronic, disabling, conditions. Strengthening the community based interventions by training community workers under supervision in line with what is envisaged in the National Mental Health Programme which was launched in 1982.

We are also aware that the trial on which this intervention is based is a relatively small pilot study; we strongly advocate for a multi-center trial which can evaluate the feasibility, acceptability and effectiveness of this intervention in diverse settings in the country. Future research should also examine the possibility of replacing the psychiatrist (a scarce resource in many parts of India) by the general practitioner trained in dementia care. Several National Health programmes like the Revised National Tuberculosis Control programme are testimony to the fact that the medical doctor involved in the primary health care can be trained to manage serious illnesses affecting the community.

 
   References Top

1.Ferri CP, Prince M, Brayne C, Brodaty H, Fratiglioni L, Ganguli M, et al . Global prevalance of dementia: a Delphi consensus study. Lancet 2005;366:2112-7.  Back to cited text no. 1  [PUBMED]  [FULLTEXT]
2.Available from: http:/www.censusindia.net. Census 2001(date: September 2008).   Back to cited text no. 2    
3.Patel V, Prince M. Ageing and mental health in a developing country: who cares? Qualitative studies from Goa, India. Psychol Med 2001;31:29-38.  Back to cited text no. 3    
4.Varghese M, Patel V. The Graying of India. In: Agarwal S, Goel D, Salhan R, Ichhpujani R, Shrivastava S, editors. Mental Health: an Indian Perspective 1946-2000. New Delhi: Elsevier; 2004. p. 240-8.  Back to cited text no. 4    
5.Dias A, Samuel R, Patel V, Prince M, Parameshwaran R, Krishnamoorthy ES. The impact associated with caring for a person with dementia: a report from the 10/66 Dementia Research Group′s Indian network. Int J Geriatr Psychiatry 2004;19:182-4.  Back to cited text no. 5  [PUBMED]  [FULLTEXT]
6.Chandra V, Pandav R, Laxminarayan R, Tanner C, Manyam B, et al . Neurological dosorders In: Disease Control Policies related to mental, neurological, developmental and substance abuse disorders. Geneva, World Health Organisation. 2008 p. 21-37.  Back to cited text no. 6    
7.Dias A, Dewey ME, D′Souza J, Dhume R, Motghare DD, Shaji KS, et al . The effectiveness of a home care program for supporting caregivers of persons with dementia in developing countries: a randomised controlled trial from Goa, India. PLoS ONE 2008;3:e2333.  Back to cited text no. 7  [PUBMED]  [FULLTEXT]
8.Saxena S, Thornicroft G, Knapp M, Whiteford H. Resources for mental health: scarcity, inequity, and ineffi ciency. Lancet 2007;370:878-89.  Back to cited text no. 8  [PUBMED]  [FULLTEXT]
9.Prince M, Livingston G, Katona C. Mental health care for the elderly in Low income countries: A Health systems approach. World Psychiatry 2007;6:5-13.  Back to cited text no. 9  [PUBMED]  [FULLTEXT]
10.Neurological Disorders - Public Health Challenges: Dementia.Geneva, World Health Organisation 2006 Ch 3.1, 42-55  Back to cited text no. 10    
11.The World Health Report 2001 - Mental health: new understanding, new hope. Geneva, World Health Organization, 2001.  Back to cited text no. 11    

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Correspondence Address:
Amit Dias
Department of Preventive Medicine, Goa Medical College, Bambolim Goa, India

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